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作 者:丁浩然[1] 金焱[1] 浦长春 于忠臣[1] 韩立杰[1] 王弘珺[1]
机构地区:[1]吉林医药学院,吉林吉林132013
出 处:《中国民康医学》2014年第21期1-2,5,共3页Medical Journal of Chinese People’s Health
基 金:吉林省科技厅资助项目(20130101140JC);吉林省大学生创新创业训练计划项目(2013)
摘 要:目的:探讨姜黄素对Jurkat细胞增殖及凋亡的影响。方法:体外培养条件下,用姜黄素处理Jurkat细胞12h后,MTT法检测细胞的生存率和IC50值;Hoechst33342染色观察细胞凋亡的形态变化;流式细胞学检测细胞凋亡率。结果:体外培养条件下,姜黄素对Jurkat细胞的增殖有明显抑制作用,呈剂量依赖性,IC50值为31μmol/L。激光共聚焦扫描显微镜观察,随着姜黄素浓度的增加,Jurkat细胞凋亡增多。流式细胞学分析表明,低浓度姜黄素使Jurkat细胞发生早期凋亡,高浓度姜黄素使Jurkat细胞出现晚期凋亡。结论:姜黄素明显抑制Jurkat细胞增殖,同时诱导Jurkat细胞发生凋亡。Objective:To investigate effect of curcumin on proliferation and apoptosis of Jurkat cells. Methods:Under in vitro conditions, Jurkat cells were treated with different concentrations of curcumin for 12h. The cells were harvested for MTT analysis (sur-vival rate and IC50). Meanwhile, the apoptosis cells were determined with Hoechst33342 staining for morphologic changes and flow cytometry for apoptotic rate. Results: The proliferation of Jurkat cells was obviously inhibited in a dose-dependent manner ( IC50=31μmol/L) by curcumin under the in vitro conditions. The number of apoptosis cells increased with the concentration of curcumin un-der confocal laser microscope. After analyzed with flow cytometry, it found that early apoptosis cells were more in lower curcumin con-centration, and late apoptosis cells were much more in higher curcumin concentration. Conclusions:Curcumin inhibits the proliferation of Jurkat cells and induces apoptosis of Jurkat cells.
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